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It really doesn't work that way. Wait to comment after you've filled out the FAFSA and the CSS. |
BINGO. And four elderly parents in different stages of care. That is America today. But according to the FAFSA and the CSS they make too much money so must pay full=freight. Why do you not know this? |
Everyone has to make hard choices. He chose to support his parents, and not save for college. Although he is apparently cash-flowing graduate school, so perhaps you should direct your sympathy elsewhere, and not to the Harvard law grad who makes a truckload of money, can get his kid a special senatorial internship, has enough $$ to pay for multiple graduate programs at the same time, and intends to foot the bill for his kid to go to Harvard law? Surely we can agree in that on the master list of "people who deserve help to pay for their kids' college" he ranks pretty far down on the list? FFS, people, use your heads, and read. |
We did exactly the same for our two SN kids when we got the early diagnoses. Fortunately. the trusts (not huge) allowed for it. The costs were $3K every three years for testing, then private tutoring several days a week. Therapy for one, Psychiatry and meds (not covered by our health care plan) for another child. For her, over time, we went through five psychiatrists. Private SN schools at full tuition. Testing and evaluation for extra time on the ACT. ACT prep. College counseling for SN schools. Getting in to colleges that had good disability services departments. Dealing with children's numerous meltdowns at college. Then meeting with the office of disability services when they had not followed through with promised accommodations for children. By then the college trust funds were long gone. Fortunately, DW is a lawyer who had helped draft amendments to the Americans with Disabilities Act so knew her stuff, but it really was hell and FULL PAY to get our kids through college. If you haven't been there don't judge because you have no idea how difficult it is. We paid full freight at both colleges for both children because our saved assets were long gone taking care of them. But are they fully employed? YES! Can they drive (don't laugh - that's a big issue for some SN kids). YES! Do they have a 104K and employer health insurance? YES! So they can both support themselves and not have to live in a SN group home. But damn it cost a lot of money, diligence and time to get there. But my DW and I can die knowing we did our very best for our children and that they are producers in society and will not have to live off of welfare. |
I assume this is ignorance and sarcasm. All the "mommy got me an IEP to get extra time on the SAT in the world" will not get you to Oxford. Anyhow, if PP knew anything about SN kids they would know that SN kits perform better on the ACT, not the ACT. He would also know that SN schools do not have IEPS. He would also know that ACT scores do not get you accepted three years later into Oxford for summer study. All the skills build on earlier skills. If you get early testing, early evaluation, early tutoring and SN schools for the particular need, your child MAY overcome some of their learning disabilities. Of course it all depends on the particular type of learning disability and degree. But all of this costs big bucks. BIG bucks. |
Meant 401K. Dad is dyslexic too |
Bravo or Brava as the case may be! All true! But a lot of parent intervention is needed to find those right SN schools, consultants, and therapies. |
That's not what he said. He said he started saving when the children were born. How many parents do that? He said the kids are not yet at the grad school/ law school level. What do you expect him to do with the four elderly parents in the meantime? Throw them out on the street? |
I'd like to know the doctor that all these people are getting extra SAT time. We've fought the school for years and finally gave up. We, like others, spent a small fortune out of pocket in therapies, a few years of private school, etc. for our child and we cannot get any supports but 30 minutes of group speech therapy that was not related to my child's needs. School wanted to change diagnosis to support their demand for extra staffing but refused regardless of the results to give more services or supports to our child. We don't expect any help for college. Ours know they will go to a state school except if they get financial aid. |
We did that. We opened up the prepaid college plan a few months after each child was a few months old. We paid it like a car note. |
No. But that doesn't mean he deserved aid for his kids' college, either. I'm not prepared to entertain whining/complaining about "how come *we* don't get any help" from a Harvard trained lawyer who had sufficient resources to pay for the medical care of 3 parents, private school for his kids, $30k in property taxes, and still cash flow college and graduate school for his kids - and still plans to pay, as he tells in, $300k for Harvard law. This guy is in no universe a donut hole family, and it's offensive that he's asserting that he is. |
So, you had sufficient resources to pay full freight for college - and that is after paying full tuition at private schools, private tutoring, testing for extra time, college counseling, and ACT prep? Sounds like you're pretty rich. And don't need aid, and certainly aren't a donut family. |
| There are times when I have mixed feelings about having only one child, and later in life. But reading this thread is not one of those times. |
| You all need to stop beating up on this one parent. You have NO idea how little you know about parenting a child with SNs and how ignorant you all sound. In the words of Donald Rumsfeld, you don’t even know what you don’t know. For you, these are the unknown unknowns. (Kudos to you. No hard feelings. But you just do not know of which you speak.). But good on ya for thinking you were good planners. |